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Clinical Trials/NCT04991935
NCT04991935
Completed
Phase 3

A Phase 3, Multicenter, Multinational, Open-Label Extension Study to Evaluate the Long-Term Safety of CC-93538 in Adult and Adolescent Subjects With Eosinophilic Esophagitis

Celgene334 sites in 1 country367 target enrollmentAugust 9, 2022
InterventionsCC-93538

Overview

Phase
Phase 3
Intervention
CC-93538
Conditions
Eosinophilic Esophagitis
Sponsor
Celgene
Enrollment
367
Locations
334
Primary Endpoint
Incidence of Adverse Events (AEs)
Status
Completed
Last Updated
26 days ago

Overview

Brief Summary

This study is an open-label, uncontrolled study design to evaluate the long-term safety and tolerability of treatment with CC-93538. The study will enroll participants who participated in the CC-93538-EE-001 or CC-93538-DDI-001 studies.

Registry
clinicaltrials.gov
Start Date
August 9, 2022
End Date
August 14, 2025
Last Updated
26 days ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Celgene
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Previously participated in prior clinical study CC-93538-EE-001 and either:
  • Subject experienced a severe EoE flare requiring endoscopic intervention and/or concomitant rescue therapy during the Induction Phase and has completed Week 24 of the Induction Phase; OR
  • Subject completed the Induction Phase and does not qualify for entry to the Maintenance Phase for reasons other than a severe EoE flare; OR
  • Subject experienced a severe EoE flare requiring endoscopic intervention and/or concomitant rescue therapy during the Maintenance Phase and completed Week 48 of the Maintenance Phase; OR
  • Subject completed Week 48 of the Maintenance Phase
  • OR Subject must have participated in Study CC-93538-DDI-001 and completed assessments through the end of treatment visit
  • Demonstrated ≥ 80% and ≤ 120% overall compliance with required investigational product dosing during the prior studies.
  • Did not permanently discontinue investigational product in the prior studies and/or did not experience any clinically significant adverse events related to Investigational Product that would preclude further dosing in the opinion of the Investigator.
  • Females of childbearing potential must have a negative pregnancy test prior to the first dose of open-label CC-93538 and agree to practice a highly effective method of contraception (as defined in the prior study) until 5 months after the last dose of open-label CC-93538.

Exclusion Criteria

  • Clinical or endoscopic evidence of other diseases or conditions that may affect or confound the histologic, endoscopic, or clinical symptom evaluation for this study.
  • Active Helicobacter pylori infection or esophageal varices.
  • Evidence of immunosuppression, or of having received systemic immunosuppressive or immunomodulating drugs within 5 drug half-lives prior to open-label extension study (OLE) Day
  • Use of these agents is prohibited during the study.
  • Treatment with oral or sublingual immunotherapy within 6 months of OLE Day
  • Use of these agents is prohibited during the study.
  • Received an investigational product, other than that administered in the CC-93538-EE-001 or CC-93538-DDI-001 studies, within 5 half-lives prior to OLE Day 1 (includes investigational product received during an interventional trial for COVID-19). Those vaccinated with an investigational COVID-19 vaccine during the CC-93538-EE-001 or CC-93538-DDI-001 studies are not eligible to participate, unless allowed following a discussion with the Clinical Trial Physician.
  • Received a live attenuated vaccine within one month prior to OLE Day 1; or anticipates the need for a live attenuated vaccine at any time throughout the course of this study.
  • Any disease that would affect the conduct of the protocol or interpretation of the study results, or would put a patient at risk by participating in the study (e.g. colitis, celiac disease, Mendelian disorder associated with EoE, severe uncontrolled asthma, infection causing eosinophilia, hypereosinophilic syndrome, or cardiovascular condition, or neurologic or psychiatric illness that could compromise the participant's ability to accurately document symptoms of EoE; newly diagnosed malignancy, lymphoproliferative disease, or clinically significant laboratory abnormality).
  • Active parasitic/helminthic infection or a suspected parasitic/helminthic infections or chronic infection (viral hepatitis, tuberculosis, or HIV)

Arms & Interventions

Administration of CC-93538

Participants are administered CC-93538 dose subcutaneously once weekly

Intervention: CC-93538

Outcomes

Primary Outcomes

Incidence of Adverse Events (AEs)

Time Frame: For a minimum of 28 months

An AE is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values regardless of etiology. Any worsening (i.e., any clinically significant adverse change in the frequency or intensity of a preexisting condition) should be considered an AE.

Number of Participants With Treatment Emergent Adverse Events (TEAE)

Time Frame: From first dose until study completion, early discontinuation, or loss of follow up, whichever occurs first (Up to approximately 36 months)

An Adverse Event (AE) is defined as any new untoward medical occurrence or worsening of a pre-existing medical condition in a clinical investigation participant administered study treatment and that does not necessarily have a causal relationship with this treatment. A Serious Adverse Event (SAE) is defined as any untoward medical occurrence that, at any dose results in death, is life-threatening, requires inpatient hospitalization or causes prolongation of existing hospitalization.

Number of Participants With Clinically Significant Maximum Post Baseline Shifts in Laboratory Parameters

Time Frame: From first dose until study completion, early discontinuation, or loss of follow up, whichever occurs first (Up to approximately 36 months)

Blood samples were collected to assess clinical significant shifts in laboratory parameters. "Normal to High" means at baseline the value is Normal and maximum post baseline value is High.

Number of Participants With Clinically Meaningful Mean Changes in Vital Signs and Physical Parameters

Time Frame: From first dose until study completion, early discontinuation, or loss of follow up, whichever occurs first (Up to approximately 36 months)

SBP (Systolic blood Pressure) and DBP (Diastolic Blood Pressure) measured in mmHg and Heart rates measured in beats per minute.

Secondary Outcomes

  • Immunogenicity of CC-93538 assessed through the incidence of anti-drug antibodies(For a minimum of 28 months)
  • Number of Participants With Incidence of Treatment Emergent Anti-CEN Antibodies(From first dose until study completion, early discontinuation, or loss of follow up, whichever occurs first (Up to approximately 36 months))

Study Sites (334)

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